Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.128845235G>A | CA369198002 | FLNC | c.3770G>A (p.Gly1257Glu) | |
7 | g.128845235G>C | CA369198000 | FLNC | c.3770G>C (p.Gly1257Ala) | |
7 | g.128845235G>T | CA369197999 | FLNC | c.3770G>T (p.Gly1257Val) | |
7 | g.128845236G>A | CA4475119 | FLNC | c.3771G>A (p.Gly1257=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.128845236G>C | CA457579385 | FLNC | c.3771G>C (p.Gly1257=) | |
7 | g.128845236G= | CA1742585452 | FLNC | c.3771G= (p.Gly1257=) | |
7 | g.128845236G>T | CA457579388 | FLNC | c.3771G>T (p.Gly1257=) | |
7 | g.128845237C>A | CA369198012 | FLNC | c.3772C>A (p.Pro1258Thr) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.128845237C= | CA1742585460 | FLNC | c.3772C= (p.Pro1258=) | |
7 | g.128845237C>G | CA369198014 | FLNC | c.3772C>G (p.Pro1258Ala) | |
7 | g.128845237C>T | CA4475120 | FLNC | c.3772C>T (p.Pro1258Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128845238C>A | CA369198020 | FLNC | c.3773C>A (p.Pro1258His) | |
7 | g.128845238C= | CA1742585461 | FLNC | c.3773C= (p.Pro1258=) | |
7 | g.128845238C>G | CA369198022 | FLNC | c.3773C>G (p.Pro1258Arg) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.128845238C>T | CA369198025 | FLNC | c.3773C>T (p.Pro1258Leu) | gnomAD v4 |
7 | g.128845239T>A | CA457579403 | FLNC | c.3774T>A (p.Pro1258=) | gnomAD v4 |
7 | g.128845239T>C | CA457579407 | FLNC | c.3774T>C (p.Pro1258=) | |
7 | g.128845239T>G | CA457579405 | FLNC | c.3774T>G (p.Pro1258=) | |
7 | g.128845240G>A | CA369198028 | FLNC | c.3775G>A (p.Gly1259Ser) | |
7 | g.128845240G>C | CA369198031 | FLNC | c.3775G>C (p.Gly1259Arg) | |
7 | g.128845240G>T | CA369198033 | FLNC | c.3775G>T (p.Gly1259Cys) | |
7 | g.128845241G>A | CA369198036 | FLNC | c.3776G>A (p.Gly1259Asp) | ClinVar |
7 | g.128845241G>C | CA369198039 | FLNC | c.3776G>C (p.Gly1259Ala) | |
7 | g.128845241G>T | CA369198042 | FLNC | c.3776G>T (p.Gly1259Val) | |
7 | g.128845242T>A | CA457579412 | FLNC | c.3777T>A (p.Gly1259=) | |
7 | g.128845242T>C | CA457579414 | FLNC | c.3777T>C (p.Gly1259=) | |
7 | g.128845242T>G | CA457579417 | FLNC | c.3777T>G (p.Gly1259=) | |
7 | g.128845243G>A | CA4475121 | FLNC | c.3778G>A (p.Val1260Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.128845243G>C | CA369198046 | FLNC | c.3778G>C (p.Val1260Leu) | |
7 | g.128845243G= | CA1742585465 | FLNC | c.3778G= (p.Val1260=) | |
7 | g.128845243G>T | CA369198047 | FLNC | c.3778G>T (p.Val1260Phe) | |
7 | g.128845244T>A | CA369198052 | FLNC | c.3779T>A (p.Val1260Asp) | |
7 | g.128845244T>C | CA369198056 | FLNC | c.3779T>C (p.Val1260Ala) | |
7 | g.128845244T>G | CA369198058 | FLNC | c.3779T>G (p.Val1260Gly) | |
7 | g.128845245T>A | CA457579428 | FLNC | c.3780T>A (p.Val1260=) | |
7 | g.128845245T>C | CA457579429 | FLNC | c.3780T>C (p.Val1260=) | |
7 | g.128845245T>G | CA457579431 | FLNC | c.3780T>G (p.Val1260=) | |
7 | g.128845246G>A | CA4475122 | FLNC | c.3781G>A (p.Glu1261Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.128845246G>C | CA369198063 | FLNC | c.3781G>C (p.Glu1261Gln) | ClinVar dbSNP gnomAD v4 |
7 | g.128845246G= | CA1742585470 | FLNC | c.3781G= (p.Glu1261=) | |
7 | g.128845246G>T | CA369198066 | FLNC | c.3781G>T (p.Glu1261Ter) | |
7 | g.128845247A>C | CA369198068 | FLNC | c.3782A>C (p.Glu1261Ala) | |
7 | g.128845247A>G | CA369198071 | FLNC | c.3782A>G (p.Glu1261Gly) | |
7 | g.128845247A>T | CA369198074 | FLNC | c.3782A>T (p.Glu1261Val) | |
7 | g.128845248G>A | CA457579449 | FLNC | c.3783G>A (p.Glu1261=) | ClinVar dbSNP |
7 | g.128845248G>C | CA369198079 | FLNC | c.3783G>C (p.Glu1261Asp) | |
7 | g.128845248G= | CA1742585480 | FLNC | c.3783G= (p.Glu1261=) | |
7 | g.128845248G>T | CA369198082 | FLNC | c.3783G>T (p.Glu1261Asp) | |
7 | g.128845249C>A | CA369198092 | FLNC | c.3784C>A (p.Pro1262Thr) | |
7 | g.128845249C>G | CA369198089 | FLNC | c.3784C>G (p.Pro1262Ala) |